A deep learning approach to automate refinement of somatic variant calling from cancer sequencing data

We also acknowledge L. Trani for performing manual review and for valuable discussion on the project. The authors also thank the patients and their families for their selfless contribution to the advancement of science. Part of this work was performed as part of the Washington University School of Medicine Genomics Tumor Board, which was funded with private research support from the Division of Oncology and the McDonnell Genome Institute. E.K.B. was supported by the National Cancer Institute (T32GM007200 and U01CA209936). T.E.R. received support from the National Institutes of Health/National Cancer Institute (NIH/NCI) (R01CA142942) and the Breast Cancer Research Foundation.